Medtronic Sofamor Danek USA, Incorporated
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K152604 | KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw Set | January 6, 2016 |
| K150200 | CD HORIZON Growth Rod Conversion Set | February 25, 2015 |